Quality control inspector jobs in Raymond, NH - 332 jobs

Title: QC Investigations Specialist Employment Type: Contract Status: Accepting Candidates About the role This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You'll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance. Key Responsibilities • Triage manufacturing issues and lead analytical investigations and root cause analysis. • Write clear, compliant quality documentation including deviations and CAPAs. • Coordinate with SMEs to determine immediate actions, containment, and impact assessments. • Interpret data to support structured problem-solving and continuous improvement. • Provide technical operations support across manufacturing and QC functions. Qualifications • 6+ years pharmaceutical or biotech manufacturing experience. • 4+ years analytical investigation and QC-focused experience. • Strong background in RCA, deviation management, and GxP documentation. • Ability to interpret analytical data and think scientifically under time-sensitive conditions. • Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams. Compensation (MA Pay Transparency): • Estimated hourly range: $50-$55/hr (W-2). • Final rate within this range will be based on skills, experience, and interview results.

Our client is looking to bring on a Mechanical Inspector. This is a 1st shift direct hire opportunity with a 4 day work week and overtime. Responsibilities Perform detailed dimensional inspections on manufactured components utilizing precision measuring instruments such as bore gauges, micrometers, calipers, and coordinate measuring machines. Interpret engineering drawings, schematics, blueprints, and GD&T specifications to ensure accurate measurement setups. Conduct quality inspections in accordance with ASME codes & standards and ISO 13485 requirements for medical device manufacturing. Collaborate with manufacturing teams to troubleshoot measurement issues and improve inspection processes. Maintain accurate documentation of inspection results and ensure traceability in compliance with ISO 9001 and AS9100 standards. Support calibration and maintenance of measurement equipment to uphold calibration standards. Assist in root cause analysis for quality issues related to dimensional discrepancies or tooling defects. Skills Experience in Mechanical Inspectors, Quality Inspections and Quality audits. Proficiency in CMM programming using PC-DMIS or Calypso software. Strong knowledge of quality control principles, quality inspection techniques, and quality assurance practices. Familiarity with ISO 9001, AS9100, ISO 13485 standards, and ASME codes & standards. Experience with blueprint reading, GD&T, and schematic interpretation

Quality Control Inspector (CWI) Base Salary: $40-55/hr About the Role Seeking a qualified Quality Control Inspector (CWI) to ensure all structural steel fabrication meets applicable codes, standards, and client specifications. This position is responsible for visual and dimensional inspection of welded products, documenting results, and coordinating with production and QA management to maintain top-tier quality standards. Key Responsibilities Conduct visual and dimensional inspections of structural steel components. Verify welding procedures, materials, and tolerances meet AWS/CWB and project standards. Complete inspection and test plans, weld maps, and related documentation. Perform NDT (VT/MT/PT/UT) if qualified and record results. Communicate with production, supervisors, and QA Manager to resolve issues. Support training and mentorship of team members in QC practices. Qualifications CWI certification required (active and in date). Minimum 5 years of welding or QC experience in a structural steel environment. Strong understanding of AWS, AISC, and fabrication tolerances. Ability to read shop drawings, measure accurately, and complete QA forms. Experience with coatings, traceability, and documentation processes preferred. Able to lift up to 60 lbs and work both independently and as part of a team.

Quality Inspector III - Weekdays About Us Founded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, our client is reshaping how the world manufactures critical products. They build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through vertically integrated capabilities, including scalable additive manufacturing and precision machining, they deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Their team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. They foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because diverse perspectives lead to better outcomes. Job Purpose As a Quality Inspector III at our client, you will work in a diversified role within the Quality Inspection team dedicated to ensuring every product delivered meets the highest standards of precision, safety, and reliability. By applying expertise in inspection methods, quality systems, and problem-solving, this role safeguards customer trust, drives continuous improvement, and supports innovation in metal additive manufacturing. This position operates on the weekday shift: Monday-Friday, 6:00 AM to 2:30 PM. Key Responsibilities Perform First Article Inspections (FAI) and routine part inspections using calipers, micrometers, and other gauges. Verify that materials, equipment, processes, and products comply with quality specifications. Develop and validate inspection and test methods; assist in creating SOPs and inspection protocols. Monitor, analyze, and report on product quality metrics. Support compliance with customer, internal, and industry requirements (AS9100, ISO 9001, ISO 13485) through audits and gap analysis. Assist in developing and implementing process controls, corrective actions, and continuous improvement initiatives. Ensure workflows, processes, and products comply with safety regulations. Investigate and troubleshoot product or production issues. Inspect manufactured parts, issue non-conformance reports, and facilitate MRB hardware disposition and corrective action tasks. Work independently and manage daily priorities with minimal supervision. Communicate and collaborate with operations personnel to ensure production needs are met. Initiate and communicate identified nonconformances. Qualifications 5+ years of experience performing part inspections with strong drawing interpretation skills. Extensive knowledge of GD&T principles. Experience with First Article Inspections (FAI), Test Method Validation (TMV), and developing inspection methods. Proficiency in AQL sampling techniques. Skilled in performing dimensional and visual inspections. Experience with root cause analysis, data analysis, and troubleshooting. Experience in medical device, aerospace, or defense manufacturing required. Hands-on experience with advanced inspection equipment and software, including CMMs, PCMMs, vision systems, profilometers, and blue-light scanners (e.g., Zeiss, Faro, Keyence). Ability to troubleshoot issues encountered with inspection equipment. Self-motivated, hands-on team player with excellent communication skills; adaptable to fast-paced environments and excited by new challenges in metal additive manufacturing.

Primary Skills: Robotics testing (Expert), Automaton Testing (Proficient), Documentation (Proficient), Test Plans (Proficient), bug management (Proficient), Contract Type: W2 Duration: 6+ months with possible extension Pay Range: $45.00 - $50.00 per hour #LP Job Summary: We are looking for a Quality Assurance Technician II to join our team, dedicated to operating and supporting robotic technology at sortation centers. This role involves executing test plans, collecting and analyzing data, and reporting results under the guidance of Test Engineers and Engineering Leads. The successful candidate will work closely with sortation center personnel to ensure the successful integration of new technologies into our product development process. Key Responsibilities: Execute test plans developed by Global Engineering Test Engineers. Collect and analyze data from testing processes to identify areas for improvement. Engage with Test Engineers, TE Manager, and Engineering Leads for guidance and direction. Collaborate with local sortation site personnel including Operations, RME, WHS, etc. Report results and findings to stakeholders and suggest recommendations for enhancements. Must Have Skills: Operate and test robotic technologies at sortation centers, supporting onboarding into RDPI's product development process Execute engineering test plans and test cases developed by RDPI Global Engineering Test Engineers Collect, analyze, and report test data and results with accuracy and clarity Work under direct guidance from Test Engineers, TE Managers, and Engineering Leads to support testing objectives This role offers the chance to work with cutting-edge robotic technologies and contribute to the development of new processes within a leading global company. If you are passionate about quality assurance and have a knack for working with innovative technologies, we'd like to hear from you. ABOUT AKRAYA Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment. Most recently, we were recognized Inc's Best Workplaces 2024 and Silicon Valley's Best Places to Work by the San Francisco Business Journal (2024) and Glassdoor's Best Places to Work (2023 & 2022)! Industry Leaders in IT Staffing As staffing solutions providers for Fortune 100 companies, Akraya's industry recognitions solidify our leadership position in the IT staffing space. We don't just connect you with great jobs, we connect you with a workplace that inspires! Join Akraya Today! Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!

A recognized pharma company is actively seeking a new Quality Control (QC) Analyst for a great entry-level position with their QC Bioassay group. In this role, the QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents Support method transfer, qualification of critical reagents, and other assay-related activities Participate in the review and basic trending of QC data Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking Collaborate with internal teams and external partners as part of cross-functional project support Contribute to investigations and deviation reports under guidance Perform other duties, as needed Qualifications: Bachelor's Degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field Familiarity with basic Lab techniques and Data Analysis methods Strong organizational, communication, and interpersonal skills Detail-oriented and eager to develop problem-solving skills in a regulated lab environment Enthusiasm for learning and the ability to work both independently and within a team Desired Skills: Academic or internship experience with Mammalian Cell Culture and/or ELISAs

Standex International is a global industrial growth company operating through our market-leading brands in electronics, cutting-edge forming technologies, engraving and scientific refrigeration. We work with our customers to advance progress through innovation. From inventing and producing parts for next-generation space vehicles, to evolving vaccine refrigeration, designing functional textures for everyday products, improving renewable energy technology and much more, we are focused on making what's next possible. The mission of the Standex Engineering Technologies Group (ETG), through its Spincraft business, is to utilize cutting-edge technologies and processes to deliver advanced metal forming solutions to leading OEMs and Tier-1 manufacturers. These capabilities, combined with industry partnerships and unparalleled customer intimacy, allow us to design and manufacture cost-effective, single-source, quality solutions for the diversified markets of aviation, space systems, defense, energy, and medical systems. What You'll Do Read and utilize all measuring instruments common to our operations, such as rules, squares, circumference tapes, vernier tapes, vernier calipers, depth and diameter gauges, radius gauges, vide-gauge, pressure gauges, etc., with no supervision Apply all testing and measuring procedures with no supervision. Check all dimensions on spun, machined, welded, forged, cast parts, etc., and make necessary reports on inspection copy of work order. Assist the operator or supervisor in arriving at quality standards required, and make suggestions and recommendations whenever possible. Instruct others assigned to inspection in proper procedures on all types of items, and assume responsibility to spot check to determine whether work is being done properly. Assume responsibility for stopping operations on parts produced that are not within tolerances or quality standards, and report at once to supervisor and general supervisor if necessary to the worker's own superior as well. Make inspection and report all defects on incoming materials, tools, dies, casting, etc., as assigned by supervisor, and perform all inspections and related functions. Build all necessary inspection setups, gauges, fixtures, etc., without assistance, if necessary, to the fullest extent of facilities available Assume complete responsibility for the quality of work done by other inspectors and the general quality of parts shipped to customers. Always maintain the inspection department in a neat and orderly condition and exercise proper practices in the care of all equipment. Cooperate with management in observance of procedures and maintaining records required. These may be in accordance with MIL-Q-9858, or to any other specification that Spincraft must conform to What You'll Bring Certified Welding Inspector Level II Penetrant Certification Level II Eddy Current Certification Level II Ultrasonic Testing Certifications What We Value Be dependable, work well with others, and focus on the job being done Be neat and orderly around the work area Equal Opportunity Employer. We consider candidates regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. The Role The Research Associate/Quality Engineer will be responsible for performing mechanical testing of materials and components using instruments such as Mecmesin, Instron, or equivalent force-measurement systems. This role will support tensile, compression, shear, puncture, and force displacement characterization to ensure product performance, robustness, and compliance with internal quality standards. In addition, the individual will contribute to method development, qualification activities, and routine QC release testing to support clinical and commercial manufacturing programs. This is a unique opportunity to be part of an emerging early-phase clinical company bringing innovative technology to the global market. Key Responsibilities Essential duties and responsibilities include the following. Other duties may be assigned. Perform mechanical testing of materials, components, and finished MAP products using Mecmesin, Instron, or comparable systems, including tensile, compression, shear, puncture, and force displacement profiling. Develop, optimize, and maintain mechanical test methods to support product characterization, comparability studies, and design verification/validation activities. Execute routine QC mechanical release testing aligned with cGMP expectations and data integrity standards. Troubleshoot mechanical testing issues, support instrumentation maintenance, and ensure proper calibration and documentation Analyze mechanical test data, prepare technical reports, and document all activities in audit-ready laboratory records. Collaborate cross-functionally with QC, Analytical Development, Process Development, Manufacturing, and Regulatory teams to enable program success. Assist in broader QC testing efforts as needed, including support for analytical, functional, and stability assays. Independently author method SOPs, analytical protocols, technical reports, and contribute to regulatory submissions. Maintain rigorous laboratory documentation and complete, audit-ready analytical records. Collaborate effectively with QC, Manufacturing, Process Development, and Regulatory teams to enable program success across phases. Thrive in a fast-paced, cross-functional environment with excellent communication and organizational skills. Qualifications Bachelor's degree in Mechanical Engineering, Materials Science, Biomedical Engineering, or a related discipline; 1-3 years of relevant mechanical testing or QC experience, or a master's degree with applicable laboratory experience. Hands-on experience with mechanical testing instruments such as Mecmesin, Instron, Texture Analyzer, or equivalent force-measurement systems. Demonstrated proficiency in tensile, compression, shear, puncture, and force-displacement mechanical characterization. Experience developing, optimizing, and/or qualifying mechanical test methods for materials, components, or finished products. Familiarity with GMP, GLP, or ISO 17025 laboratory environments and strong understanding of data integrity (ALCOA+). Ability to analyze mechanical test data, generate clear technical reports, and maintain accurate documentation. Experience supporting QC release testing, method qualification, method transfer, or equipment qualification is a plus. Strong organizational skills with the ability to manage multiple workflows and prioritize effectively in a fast-paced environment. Excellent verbal and written communication skills and comfort working within interdisciplinary teams. Commitment to collaborative work within interdisciplinary project teams. At Vaxess, we're bringing together exceptional talent to drive our product development forward. We value collaboration, curiosity, and a dynamic work environment. To apply, please submit your CV/resume to ****************** .

Job DescriptionDEKA R&D has an immediate opening for a Quality Control Inspector to work in a dynamic Medical Device Research and Development company. This position is a highly visible role with significant and direct impact on the development and success of multiple engineering projects. Responsibilities as a Quality Control Inspector: Interpret Mechanical and Electrical print reading and apply inspection best practices Operate CMM equipment and utilize various measuring tools for inspection of medical device components Communicate effectively and promptly across multiple projects to provide feedback on inspection of parts Inspect various mechanical and electrical components and assemblies through incoming inspection Interpret ASME Y14.5 and GD&T standards throughout the inspection process for compliance and best practices Provide feedback on inspection activities to improve efficient whether individually or in a cross-functional setting To be successful as a Quality Control Inspector, you will need the following qualifications: 3+ years of experience in a regulated industry CMM programming, Metrology and/or CQI certified is a plus Basic GD&T knowledge required, Advanced GD&T knowledge preferred Proficient with mechanical measuring equipment such as micrometers, calipers, optical comparator Ability to operate CMMs following precise instructions Inspection of soldered components and Printed Circuit Board (PCB) assemblies; IPC-A-610 certification preferred Computer skills and knowledge; ability to learn new software (Experience with Jira is a plus) About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored. Powered by JazzHR VAABeEHa8x

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Job Description Were seeking a Quality Mechanical Inspector to perform detailed, accurate mechanical inspections-including FAIs, Gage R&R, OQ, PQ, and IQ-to strict drawing requirements and established quality standards. This role is highly detail-oriented and requires precision, hands-on metrology experience, and the ability to document results clearly. Youll work with CMM (Hexagon PC-DMIS), optical comparator, OGP, and traditional inspection tools (calipers, micrometers, height gages, pin gages, tool mics), and complete visual inspections to established standards. Key Responsibilities Perform dimensional and visual inspections using CMM, optical comparator, calipers, micrometers, height gages, and other metrology tools. Accurately document inspection results per company inspection procedures (e.g., TechNH standards if applicable). Write basic CMM programs to measure parts for FAIs, CPKs, PQs, OQs, and IQs. Conduct FAIs and Gage R&R, as well as PQ, OQ, and IQ inspections. Utilize standardized CMM fixturing based on part geometry. Interpret ballooned customer drawings with a basic understanding of GD&T. Maintain an accurate library of programs and written setup instructions for all CMM and OGP programs. Qualifications Required: Minimum 1 year experience as a mechanical inspector. Minimum 1 year CMM experience; ability to create basic CMM programs (Hexagon PC-DMIS knowledge required). Proficiency with optical comparators, tool mics, pin gages, and related tools. Basic understanding of GD&T measurements. Proficient in Microsoft Excel and MS Office. Ability to read blueprints, inspection reports, and quality documentation. Strong communication skills; ability to work independently with minimal supervision and collaborate with engineers, shift supervisors, and machine technicians. Demonstrated ability to work effectively in a multi-discipline, collaborative environment. Experience in QMS/Regulatory environments. Preferred: Experience writing basic programs for OGP systems. Familiarity with CPK studies and data reporting. Strong presentation and reporting skills. What Youll Bring High attention to detail and a commitment to accuracy. Ability to take direction well and carry out instructions competently. A team-first mindset and clear, professional communication.

Job DescriptionBenefits: 401(k) 401(k) matching Bonus based on performance Health insurance Resin Systems is a manufacturer of custom thermoset resin castings utilizing epoxy, urethane and silicone materials designed for highly dependable performance in hundreds of demanding applications and environments. Resin Systems creates components for a wide range of industries including Semiconductor, RF Microwave and Medical. Resin Systems Corporation is looking for talented individuals to support our continued growth. We have 1st shift positions available in our QC inspection department. Quality Inspector Responsibilities: - Conduct dimensional inspections on incoming materials, in-process production, and finished products from the various product lines as assigned by supervisor/management. - Use various measuring tools and equipment such as calipers, thread gages, pins and height gages to ensure product specifications are met - Perform visual inspections to identify any cosmetic defects or non-conformities - Perform cosmetic rework on identified minor cosmetic defects - Document and report inspection results and maintain accurate records - Follow established quality control (QC) procedures and guidelines Quality Inspector Skills: - Strong knowledge of quality control principles and practices - Proficiency in using measuring tools and equipment - Attention to detail and ability to identify defects or non-conformities - Excellent analytical and problem-solving skills - Familiarity with QC (Quality Control) processes - Ability to read and interpret technical drawings and specifications - Positive attitude and strong communication skills to collaborate with cross-functional teams - Must be willing to take initiative and be a self-starter Please note that this is not an exhaustive list of responsibilities and skills. Other duties may be assigned as needed by supervisor/management based on business requirements. Job Type: Full-time 8 hour shift Day shift Monday to Friday One location Ability to lift 50 lbs

1. Qualifications: a. High school diploma or GED required b. Minimum 3 years of relevant quality experience, within ISO13485/GMP manufacturing environment preferred, within extrusion is a plus c. Demonstrated efficiency and competency in core and advanced methods and gages for the inspection of tightly toleranced products d. Ability to read and interpret Engineering drawings e. Demonstrate initiative and self-motivation to create efficiencies and improve productivity within the inspection process f. Able to adapt and apply inspection knowledge to an array of product geometries and materials g. Work independently and prioritize assignments h. Will receive ongoing training to support competency and growth within the role i. Will receive opportunity and training to support growth within QC 2. Basic Position Skills: a. Organization Able to react and maintain order and focus across shifting priorities and tasks b. Time Management Able to balances multiple responsibilities and create efficiencies within the inspection process and achieve due dates c. Critical Thinking Able to apply and adapt training and experience effectively to assigned tasks; ability to interact with data and identify risk d. Communication Able to contribute across the team and coordinate with and support others to achieve departmental goals e. Mature work ethic professional and positive attitude; provide constructive feedback and ownership to drive improvement within areas of responsibility 3. Reports to: Quality Supervisor 4. Primary job responsibility: The QC Inspector Level 2 is a mid-level position within the QC department for individuals who have demonstrated proficiency in all Level 1 competencies and responsibilities. The Level 2 Inspector utilizes core and advanced inspection methods and gages efficiently to perform inspections of extruded product across a broad range of product geometries and material to determine conformance to defined specifications. This position may include responsibility for an assigned Quality workflow and/or area of focus within an area of demonstrated expertise, efficiency and experience. 5. Essential functions of position: Perform Final Inspection for product Lot Release a. Prepare, follow, perform and document final inspections as defined on inspection paperwork for lot release b. Adapt inspection method techniques to accommodate the inspection of an array of products, including prototypes, profiles, multi-lumen and thin wall extruded tubes c. Demonstrate acceptable measurement error within inspection methods and techniques d. Assess conformance to defined specifications and requirements and identify and document non-conformance reports (NCR) e. Perform boundary inspections and actions as required to contain non-conforming product f. Complete thorough and detailed end-of-shift reporting Perform Start up and In-process inspection of manufacturing extrusion lines a. Prepare, follow and perform start-up and in-process inspections for multiple extrusion lines within a shift for an array of parts with varying degrees of difficulty relating to raw material properties, geometries, tolerances and methods b. React, adjust and communicate appropriately to challenges encountered during the extrusion process c. Identify and document non-conformances to defined specifications and requirements during the extrusion process d. Communicate inspection results and work with extrusion technician or operator to address non-conformances and at-risk product e. Identify, document, and perform boundary inspection to contain at-risk product encountered during the extrusion process Assigned Quality Workflow or Area of Focus a. Support assigned workflow or area of focus with accountability and action b. Create documented procedures and provide training as warranted c. Maintain appropriate documentation and tracking of workflow outcomes and performance as warranted d. Identify under performance and risk within the workflow and action needed to sustain and/or improve workflow outcomes and performance as warranted e. Coordinate and work with others as needed in support of assigned workflow f. Provide and maintain active communication and updates of assigned workflow to Quality Manager and/or Supervisor. Inspection Methods, Gages and Equipment a. Utilize pin gages, ring gages, calipers, rulers, vision systems, and other applicable gages as specified and within scope of training b. Utilize advanced inspection methods including automated OGP routines and advanced vision system techniques such as modeling and construction c. Recognize and respond to basic visual and dimensional quality indicators and erroneous data d. Create efficiencies within the inspection process e. Identify and report equipment and gages outside of calibration dates and exhibiting damage, wear, or malfunctions Documentation and Compliance f. Adhere to Good Documentation Practices (GDP) requirements g. Maintain accurate and complete records in all required documentation h. Follow defined processes and procedures appropriately and effectively identify gaps and/or misalignment with requirements i. Maintain product and lot traceability throughout the workflow and in all inspection documentation Safety and Housekeeping a. Follow all requirements and equipment safety procedures b. Identify and report safety hazards c. Keep work area clean and organized Communication a. Professional and courteous interactions b. Effective use of email and daily reporting to facilitate follow-up and action c. Proactive and constructive communication and support across the team to drive improvement and collaboration 6. Is the work described above checked by another individual? ? YES ? NO 7. Work Environment: a. Dynamic and fast-paced manufacturing floor, prone to interruptions b. Exposure to noise, high temperatures, moving machinery, and high-voltage equipment c. Clean room and gowning requirements * Is the work described above checked by another individual? YES * Consistent motor skills and other requirements of the position: Persistent: Standing: 10% Sitting: 75% Walking: 15% Consistent lifting of up to 35 lbs. Rarely lifting of 1 lb. Frequently Maximum carrying distance of up to 30 ft. Occasionally Reaching must be able to reach machines and/or materials up to 6 ft. from Frequently Kneeling N/A Climbing stairs N/A Repetitive motion right/left hand/wrist Frequently Repetitive motion right/left foot/ankle N/A Continuous arm motions Yes Must be able to avoid potentially moving which could cause injury Yes Must be able to grasp and move object consistently and regularly Yes Vision: intricate nature of work requires of 20/20 with or without corrective lenses Yes Must be able to use gaging equipment and tools Yes Must demonstrate to work productively and efficiently with others Yes Microspec offers competitive wages and benefits, including: Sign-On Bonus Comprehensive Health Insurance Matching 401K plan annually after 1 year Entry-level 2 weeks paid vacation 64 Hours personal/sick time (unused time paid out at the end of the year) Annual discretionary bonus Salary range-$26.50-$28.00 per hour based on experience 20% Second Shift Differential

Rennscot MFG, founded in 2017, started as a motorsports-focused shop in the aftermarket automotive industry. Now, they are a leading provider of advanced manufacturing services located in Woburn, MA. Rennscot MFG strives to be more than just a machine shop; they solve problems in innovative ways, using a suite of integrated services to fuel a passion for ideation. With a focus on diversifying into commercial and critical technology sectors, Rennscot MFG delivers cutting-edge technologies and unwavering commitment to quality. They offer a comprehensive range of services, including reverse engineering, metal & polymer additive manufacturing, and precision machining to support various industries' needs. For more information, visit rennscotmfg.com. Description The Quality Control Inspector is responsible for ensuring that manufactured components meet engineering and customer specifications through precise inspection processes. This role places a strong emphasis on visual inspections, along with manual inspection methods, and requires a keen understanding of technical drawings and GD&T. Candidates will be considered for either an L1 (entry-level) or L2 (experienced) inspector position based on experience and qualifications. Responsibilities Operate pre-programmed CMM inspections (Zeiss/Calypso preferred) Load/unload parts and verify setups Interpret CMM results and compare them against engineering requirements Document findings in the MES (ProShop) and communicate deviations Perform manual inspections using a variety of precision metrology tools Calipers, micrometers, height gauges, thread gauges, bore gauges, etc. Visual inspections for defects such as nicks, scratches, and finish inconsistencies Review technical drawings and apply GD&T principles to inspections Conduct receiving, in-process, and final inspections Assist in non-conformance investigations, root cause analysis, and corrective actions Maintain accurate inspection records and ensure compliance with AS9100/ISO9001 standards Collaborate with machinists, engineers, and quality team members to resolve inspection-related concerns Adhere to company safety protocols, including proper PPE usage (eye protection, hearing protection, etc.) Step into other support roles as needed based on company demands; assist with CNC machine operation, post-processing additively manufactured parts, mechanical assembly, or logistics tasks (e.g., driving components to/from outside processing vendors) Required Skills & Qualifications Experience in quality inspection within a manufacturing environment Strong ability to interpret technical drawings, GD&T, and work instructions Proficiency in basic metrology tools (calipers, micrometers, etc.) Familiarity with non-conformance documentation and quality reporting Attention to detail and ability to work independently in a fast-paced environment Preferred Skills & Qualifications Experience running CMM programs (Zeiss/Calypso preferred) Ability to make minor adjustments to Calypso programs Understanding of statistical process control (SPC) and quality tools (FMEA, control plans, etc.) Experience working in regulated industries (aerospace, medical, automotive, etc.) Physical Demands Standing for extended periods Lifting/moving objects up to 50 lbs Fine motor skills for handling small precision components Working in an industrial environment requiring PPE (eye protection, hearing protection, etc.) ITAR Requirement To conform to US Government export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a US citizen, lawful permanent resident of the US, protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the US Department of State. Learn more about the ITAR here: **************************************************************************************** Rennscot MFG is an Equal Opportunity Employer; employment with Rennscot MFG is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary: Verification of procured materials, sub-assemblies, finished products, and processes to the company's Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions: Inspect measure and/or test material to established methods and standards. Utilize various inspection tools, such as Rulers, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. Document inspection and test results according to established procedures. Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. Process returned material to established procedures. Read and interpret documentation such as Standard Operating Procedures (SOP), PDAs, and ECOs. Interface with other functions and departments as required. Perform other duties as assigned. Perform basic visual inspection of shipping material & products The Ability to train Inspectors on Zoll SOPs Skill Requirements: Good written and oral communication skills. Ability to read procedures Familiar with the use of mechanical and electronic test equipment. Basic computer skills: Microsoft Office, Ability to lift up to 50 lbs. Required/ Preferred Education and Experience: High school diploma or equivalent. 0 to 3 years' experience in a related position. Oracle and MES experience preferred Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities will be reviewed periodically as duties and responsibilities change with business necessities. Essential and marginal job functions are subject to modification. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990 #LI-LV1 The hourly pay rate for this position is: $18.50 to $18.50 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

Acute Care Technology At ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions. The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Products include AEDs, trauma kits, ventilators, temperature management solutions, and more. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service. At ZOLL, you won't just have a job. You'll have a career-and a purpose. Join our team. It's a great time to be a part of ZOLL! Job Summary: Verification of procured materials, sub-assemblies, finished products, and processes to the company's Quality Standards. This may include visual inspection, dimensional measurement, and electrical testing to verify conformance to established standards and specifications. Essential Functions: * Inspect measure and/or test material to established methods and standards. * Utilize various inspection tools, such as Rulers, DVMs, Power Supplies, Defib/Pacer Analyzers, custom fixtures etc. per procedures. * Document inspection and test results according to established procedures. * Maintain quality documentation files such as, Device History Records (DHR) and Inspection History Records. * Process returned material to established procedures. * Read and interpret documentation such as Standard Operating Procedures (SOP), PDAs, and ECOs. * Interface with other functions and departments as required. * Perform other duties as assigned. * Perform basic visual inspection of shipping material & products * The Ability to train Inspectors on Zoll SOPs Skill Requirements: * Good written and oral communication skills. * Ability to read procedures * Familiar with the use of mechanical and electronic test equipment. * Basic computer skills: Microsoft Office, * Ability to lift up to 50 lbs. Required/ Preferred Education and Experience: * High school diploma or equivalent. * 0 to 3 years' experience in a related position. * Oracle and MES experience preferred Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities will be reviewed periodically as duties and responsibilities change with business necessities. Essential and marginal job functions are subject to modification. ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives. ZOLL Medical Corporation appreciates and values diversity. We are an Equal Opportunity Employer M/F/D/V. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990 #LI-LV1 The hourly pay rate for this position is: $18.50 to $18.50 Factors which may affect this rate include shift, geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at ********************* Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee's primary work location. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran. ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

The Middlesex Corporation is a nationally recognized and award-winning leader in the heavy civil construction industry. Since 1972, the family business founded by Robert W. Pereira has developed an extensive client and project list through its consistent efforts to safely build America's infrastructure. The Middlesex Corporation specializes in building and reconstructing highways, bridges, marine, rail, and transit facilities through its collaborative team approach and focus on core values. In addition, Middlesex Asphalt in Central Florida is one of the largest and most productive asphalt plants in the United States with Middlesex Paving earning an equally solid regional presence and reputation. Position Summary: The MRM Quality Control Technician is responsible for ensuring the quality, consistency, and compliance of ready mixed concrete and aggregates produced by Massachusetts Ready Mix. This role performs routine plant and field testing, inspections, and documentation to verify materials meet applicable job specifications, Department of Transportation requirements, and industry standards. PI5bee3612ed65-37***********9

Summary of Primary Responsibilities: The QC Incoming Inspector completes all activities required to approve raw materials for use in product manufacture. The position also performs inspection activities during in-process manufacturing. Specific Responsibilities: Perform quality line clears and in process inspections during the inspection and packing processes according to specific SOP requirements Issue lot numbers and control labels for incoming raw materials; perform inspections per internal procedures and specifications Release approved raw materials for use in manufacturing process to include completion of associated documents, notice of approval form (bin card) and relabeling of inventory Review MPS of other incoming inspectors for approval and release. Monitor and perform annual retain inspection; coordinate required retesting with QC; complete required documentation Perform OOS investigations and participate in MRB as required for rejected materials Perform as SME for the function and provide training as required to new employees, contractors and other QA personnel Perform biennial review for designated procedures and MPS as needed Documents; author and complete DCR as required Document all work activities according to Good Documentation Practices Maintain current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Participate in other projects as assigned Job Complexity: The position works on assignments that are routine in nature and receives detailed instruction on all work. Supervisory Responsibilities: None Required Qualifications: Associates degree in the life science or relevant work experience 0 - 1 year of experience in a cGMP facility or previous experience in a QA/QC role within the industry; internship experience considered Experience using Microsoft Office or an ERP system Desired Experience, Knowledge, and Skills: Bachelor's degree preferred Experience working in a clean room environment Excellent communication and documentation skills The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Were seeking a Quality Mechanical Inspector to perform detailed, accurate mechanical inspections-including FAIs, Gage R&R, OQ, PQ, and IQ-to strict drawing requirements and established quality standards. This role is highly detail-oriented and requires precision, hands-on metrology experience, and the ability to document results clearly. Youll work with CMM (Hexagon PC-DMIS), optical comparator, OGP, and traditional inspection tools (calipers, micrometers, height gages, pin gages, tool mics), and complete visual inspections to established standards. Key Responsibilities Perform dimensional and visual inspections using CMM, optical comparator, calipers, micrometers, height gages, and other metrology tools. Accurately document inspection results per company inspection procedures (e.g., TechNH standards if applicable). Write basic CMM programs to measure parts for FAIs, CPKs, PQs, OQs, and IQs. Conduct FAIs and Gage R&R, as well as PQ, OQ, and IQ inspections. Utilize standardized CMM fixturing based on part geometry. Interpret ballooned customer drawings with a basic understanding of GD&T. Maintain an accurate library of programs and written setup instructions for all CMM and OGP programs. Qualifications Required: Minimum 1 year experience as a mechanical inspector. Minimum 1 year CMM experience; ability to create basic CMM programs (Hexagon PC-DMIS knowledge required). Proficiency with optical comparators, tool mics, pin gages, and related tools. Basic understanding of GD&T measurements. Proficient in Microsoft Excel and MS Office. Ability to read blueprints, inspection reports, and quality documentation. Strong communication skills; ability to work independently with minimal supervision and collaborate with engineers, shift supervisors, and machine technicians. Demonstrated ability to work effectively in a multi-discipline, collaborative environment. Experience in QMS/Regulatory environments. Preferred: Experience writing basic programs for OGP systems. Familiarity with CPK studies and data reporting. Strong presentation and reporting skills. What Youll Bring High attention to detail and a commitment to accuracy. Ability to take direction well and carry out instructions competently. A team-first mindset and clear, professional communication.